CA2563302A1 - Combinaisons de glycopyrrolate et d'agonistes de recepteur beta2-adrenergique - Google Patents
Combinaisons de glycopyrrolate et d'agonistes de recepteur beta2-adrenergique Download PDFInfo
- Publication number
- CA2563302A1 CA2563302A1 CA002563302A CA2563302A CA2563302A1 CA 2563302 A1 CA2563302 A1 CA 2563302A1 CA 002563302 A CA002563302 A CA 002563302A CA 2563302 A CA2563302 A CA 2563302A CA 2563302 A1 CA2563302 A1 CA 2563302A1
- Authority
- CA
- Canada
- Prior art keywords
- hydroxy
- alkyl
- optionally substituted
- alkoxy
- ethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- VPNYRYCIDCJBOM-UHFFFAOYSA-M Glycopyrronium bromide Chemical compound [Br-].C1[N+](C)(C)CCC1OC(=O)C(O)(C=1C=CC=CC=1)C1CCCC1 VPNYRYCIDCJBOM-UHFFFAOYSA-M 0.000 title claims abstract 6
- 229940015042 glycopyrrolate Drugs 0.000 title claims abstract 6
- 239000000556 agonist Substances 0.000 title 1
- 102000014974 beta2-adrenergic receptor activity proteins Human genes 0.000 title 1
- 108040006828 beta2-adrenergic receptor activity proteins Proteins 0.000 title 1
- 239000003814 drug Substances 0.000 claims abstract 17
- 150000001875 compounds Chemical class 0.000 claims abstract 6
- 208000027771 Obstructive airways disease Diseases 0.000 claims abstract 4
- 208000027866 inflammatory disease Diseases 0.000 claims abstract 4
- 230000002757 inflammatory effect Effects 0.000 claims abstract 4
- 150000003839 salts Chemical group 0.000 claims abstract 4
- 239000012453 solvate Chemical group 0.000 claims abstract 4
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 29
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 21
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 14
- 125000005843 halogen group Chemical group 0.000 claims 12
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 239000001257 hydrogen Substances 0.000 claims 11
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 10
- -1 cyano, hydroxy Chemical group 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 239000006185 dispersion Substances 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 239000000443 aerosol Substances 0.000 claims 5
- 125000004432 carbon atom Chemical group C* 0.000 claims 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 4
- 239000003937 drug carrier Substances 0.000 claims 4
- 150000002431 hydrogen Chemical group 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- 239000000843 powder Substances 0.000 claims 4
- 239000003380 propellant Substances 0.000 claims 4
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 239000002775 capsule Substances 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 2
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- JYNZIOFUHBJABQ-UHFFFAOYSA-N allyl-{6-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-hexyl-}-methyl-amin Chemical group C=1OC2=CC(OCCCCCCN(C)CC=C)=CC=C2C=1C1=CC=C(Br)C=C1 JYNZIOFUHBJABQ-UHFFFAOYSA-N 0.000 claims 2
- SYGWYBOJXOGMRU-UHFFFAOYSA-N chembl233051 Chemical group C1=CC=C2C3=CC(C(N(CCN(C)C)C4=O)=O)=C5C4=CC=CC5=C3SC2=C1 SYGWYBOJXOGMRU-UHFFFAOYSA-N 0.000 claims 2
- 238000002648 combination therapy Methods 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical group 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- GTTZQULJQRNNER-HNNXBMFYSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[(2-methyl-1-phenylpropan-2-yl)amino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NC(C)(C)CC1=CC=CC=C1 GTTZQULJQRNNER-HNNXBMFYSA-N 0.000 claims 1
- QTWVYUJFBIVOHT-RYQLBKOJSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[[(1s,2r)-2-phenylmethoxycyclopentyl]amino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound O([C@@H]1CCC[C@@H]1NC[C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)CC1=CC=CC=C1 QTWVYUJFBIVOHT-RYQLBKOJSA-N 0.000 claims 1
- QTWVYUJFBIVOHT-SZMVWBNQSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[[(1s,2s)-2-phenylmethoxycyclopentyl]amino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound O([C@H]1CCC[C@@H]1NC[C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)CC1=CC=CC=C1 QTWVYUJFBIVOHT-SZMVWBNQSA-N 0.000 claims 1
- ONNGKMAEIWXVBI-UHFFFAOYSA-N 4-hydroxy-7-[1-hydroxy-2-[2-[4-(4-phenylbutoxy)phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C=1C=C(O)C=2NC(=O)SC=2C=1C(O)CNCCC(C=C1)=CC=C1OCCCCC1=CC=CC=C1 ONNGKMAEIWXVBI-UHFFFAOYSA-N 0.000 claims 1
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims 1
- AUUXBAOWHVOGFM-FTBISJDPSA-N 5-[(1r)-2-[(5,6-diethyl-2,3-dihydro-1h-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy-1h-quinolin-2-one;hydrochloride Chemical compound Cl.N1C(=O)C=CC2=C1C(O)=CC=C2[C@@H](O)CNC1CC(C=C(C(=C2)CC)CC)=C2C1 AUUXBAOWHVOGFM-FTBISJDPSA-N 0.000 claims 1
- SXHDWOIPFGGJDK-QFIPXVFZSA-N 5-[(1r)-2-[(5,6-diethyl-2-methyl-1,3-dihydroinden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2[C@@H](O)CNC1(C)CC(C=C(C(=C2)CC)CC)=C2C1 SXHDWOIPFGGJDK-QFIPXVFZSA-N 0.000 claims 1
- BIVAGPLVSDRQHP-VZYDHVRKSA-N 5-[(1s)-2-[(4,7-diethyl-2,3-dihydro-1h-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy-1h-quinolin-2-one;hydrochloride Chemical compound Cl.N1C(=O)C=CC2=C1C(O)=CC=C2[C@H](O)CNC1CC(C(CC)=CC=C2CC)=C2C1 BIVAGPLVSDRQHP-VZYDHVRKSA-N 0.000 claims 1
- HHEMVSCLLFFBQM-UHFFFAOYSA-N 5-[2-(2,3-dihydro-1h-inden-2-ylamino)-1-hydroxyethyl]-8-hydroxy-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2C(O)CNC1CC2=CC=CC=C2C1 HHEMVSCLLFFBQM-UHFFFAOYSA-N 0.000 claims 1
- LKKKXVXXRSMKJD-UHFFFAOYSA-N 5-[2-[(5,6-diethyl-2,3-dihydro-1h-inden-2-yl)amino]-1-hydroxyethyl]-8-(methoxymethoxy)-6-methyl-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(OCOC)=CC(C)=C2C(O)CNC1CC(C=C(C(=C2)CC)CC)=C2C1 LKKKXVXXRSMKJD-UHFFFAOYSA-N 0.000 claims 1
- CEVVMMPBOCCERE-UHFFFAOYSA-N 5-[2-[(5,6-diethyl-2,3-dihydro-1h-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical compound N1C(=O)CCC2=C1C(O)=CC=C2C(O)CNC1CC(C=C(C(=C2)CC)CC)=C2C1 CEVVMMPBOCCERE-UHFFFAOYSA-N 0.000 claims 1
- LNWINKMRDGCDER-UHFFFAOYSA-N 5-[2-[(5,6-diethyl-2,3-dihydro-1h-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy-3-methyl-1h-quinolin-2-one Chemical compound N1C(=O)C(C)=CC2=C1C(O)=CC=C2C(O)CNC1CC(C=C(C(=C2)CC)CC)=C2C1 LNWINKMRDGCDER-UHFFFAOYSA-N 0.000 claims 1
- IAYCRMOPCKGMOQ-UHFFFAOYSA-N 5-[2-[(5,6-diethyl-2,3-dihydro-1h-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy-6-methyl-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(O)=CC(C)=C2C(O)CNC1CC(C=C(C(=C2)CC)CC)=C2C1 IAYCRMOPCKGMOQ-UHFFFAOYSA-N 0.000 claims 1
- ZQWNZUAMWNPQGR-UHFFFAOYSA-N 5-[2-[(5,6-diethyl-2,3-dihydro-1h-inden-2-yl)amino]ethyl]-8-hydroxy-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2CCNC1CC(C=C(C(=C2)CC)CC)=C2C1 ZQWNZUAMWNPQGR-UHFFFAOYSA-N 0.000 claims 1
- XRZOULQZLDILQH-UHFFFAOYSA-N 5-[2-[(5,6-dimethoxy-2,3-dihydro-1h-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxy-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2C(O)CNC1CC(C=C(C(=C2)OC)OC)=C2C1 XRZOULQZLDILQH-UHFFFAOYSA-N 0.000 claims 1
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims 1
- 125000001960 7 membered carbocyclic group Chemical group 0.000 claims 1
- IHAMMEZCFQUEDK-BDQAORGHSA-N 8-hydroxy-5-[(1r)-1-hydroxy-2-(6,7,8,9-tetrahydro-5h-benzo[7]annulen-7-ylamino)ethyl]-1h-quinolin-2-one;hydrochloride Chemical compound Cl.C1CC2=CC=CC=C2CCC1NC[C@H](O)C1=CC=C(O)C2=C1C=CC(=O)N2 IHAMMEZCFQUEDK-BDQAORGHSA-N 0.000 claims 1
- HKVADJQGWKQGFS-QFIPXVFZSA-N 8-hydroxy-5-[(1r)-1-hydroxy-2-[(2-methyl-1,3,5,6,7,8-hexahydrocyclopenta[b]naphthalen-2-yl)amino]ethyl]-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2[C@@H](O)CNC1(C)CC2=CC(CCCC3)=C3C=C2C1 HKVADJQGWKQGFS-QFIPXVFZSA-N 0.000 claims 1
- MXCGESVXTRYGMG-SFHVURJKSA-N 8-hydroxy-5-[(1r)-1-hydroxy-2-[(2-methyl-1,3-dihydroinden-2-yl)amino]ethyl]-1h-quinolin-2-one Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2[C@@H](O)CNC1(C)CC2=CC=CC=C2C1 MXCGESVXTRYGMG-SFHVURJKSA-N 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 claims 1
- 239000008186 active pharmaceutical agent Substances 0.000 claims 1
- 230000001387 anti-histamine Effects 0.000 claims 1
- 230000003110 anti-inflammatory effect Effects 0.000 claims 1
- 239000000739 antihistaminic agent Substances 0.000 claims 1
- 239000003434 antitussive agent Substances 0.000 claims 1
- 229940124584 antitussives Drugs 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- 229940124630 bronchodilator Drugs 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000006184 cosolvent Substances 0.000 claims 1
- 239000000850 decongestant Substances 0.000 claims 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000002552 dosage form Substances 0.000 claims 1
- 229940088679 drug related substance Drugs 0.000 claims 1
- ZEXCGJJNMGJWDF-FERBBOLQSA-N formic acid;4-hydroxy-7-[(1r)-1-hydroxy-2-[2-(5,6,7,8-tetrahydronaphthalen-2-yl)ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound OC=O.C1([C@H](CNCCC=2C=C3CCCCC3=CC=2)O)=CC=C(O)C2=C1SC(=O)N2 ZEXCGJJNMGJWDF-FERBBOLQSA-N 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- IREJFXIHXRZFER-PCBAQXHCSA-N indacaterol maleate Chemical compound OC(=O)\C=C/C(O)=O.N1C(=O)C=CC2=C1C(O)=CC=C2[C@@H](O)CNC1CC(C=C(C(=C2)CC)CC)=C2C1 IREJFXIHXRZFER-PCBAQXHCSA-N 0.000 claims 1
- 150000002688 maleic acid derivatives Chemical class 0.000 claims 1
- 229940071648 metered dose inhaler Drugs 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4704—2-Quinolinones, e.g. carbostyril
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4015—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/402—1-aryl substituted, e.g. piretanide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pulmonology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Saccharide Compounds (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Cette invention concerne un médicament comprenant, séparément ou conjointement, (A) un glycopyrrolate; et (B) soit un composé de formule (I) sous forme libre, sous forme de sel ou sous forme de solvate, dans laquelle W, R?x¿, R?y¿, R?1¿, R?2¿, R?3¿, R?4¿, R?5¿, R?6¿ et R?7¿ ont les notations indiquées dans les pièces descriptives de la demande, soit un composé de formule (II) sous forme libre, sous forme de sel ou sous forme de solvate, dans laquelle X possède la notation indiquée dans les pièces descriptives de la demande, en vue d'une administration simultanée, séquentielle ou séparée dans le traitement des maladies inflammatoires ou obstructives des voies respiratoires. Cette invention concerne également des compositions pharmaceutiques qui contiennent (A) et (B).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0411056.5A GB0411056D0 (en) | 2004-05-18 | 2004-05-18 | Organic compounds |
| GB0411056.5 | 2004-05-18 | ||
| PCT/EP2005/005354 WO2005110402A1 (fr) | 2004-05-18 | 2005-05-17 | Combinaisons de glycopyrrolate et d'agonistes de recepteur beta2-adrenergique |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2563302A1 true CA2563302A1 (fr) | 2005-11-24 |
| CA2563302C CA2563302C (fr) | 2012-08-28 |
Family
ID=32607514
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2563302A Expired - Lifetime CA2563302C (fr) | 2004-05-18 | 2005-05-17 | Combinaisons de glycopyrrolate et d'agonistes de recepteur beta2-adrenergique |
Country Status (33)
| Country | Link |
|---|---|
| US (6) | US20080267886A1 (fr) |
| EP (3) | EP2228064B1 (fr) |
| JP (2) | JP5567252B2 (fr) |
| KR (2) | KR20130018429A (fr) |
| CN (1) | CN1953745A (fr) |
| AT (1) | ATE521348T1 (fr) |
| AU (1) | AU2005244439C1 (fr) |
| BE (1) | BE2020C517I2 (fr) |
| BR (1) | BRPI0511327B8 (fr) |
| CA (1) | CA2563302C (fr) |
| CY (4) | CY1112086T1 (fr) |
| DK (2) | DK1755590T3 (fr) |
| EC (1) | ECSP066950A (fr) |
| ES (2) | ES2775979T3 (fr) |
| FR (1) | FR20C1018I2 (fr) |
| GB (1) | GB0411056D0 (fr) |
| HU (3) | HUE048936T2 (fr) |
| IL (1) | IL179013A (fr) |
| LT (3) | LT2228064T (fr) |
| LU (1) | LUC00155I2 (fr) |
| MA (1) | MA28598B1 (fr) |
| MX (1) | MXPA06013382A (fr) |
| NO (2) | NO334760B1 (fr) |
| NZ (1) | NZ550369A (fr) |
| PL (2) | PL2228064T3 (fr) |
| PT (2) | PT2228064T (fr) |
| RU (1) | RU2388465C2 (fr) |
| SE (1) | SE1755590T5 (fr) |
| SG (1) | SG153836A1 (fr) |
| SI (2) | SI2228064T1 (fr) |
| TN (1) | TNSN06377A1 (fr) |
| WO (1) | WO2005110402A1 (fr) |
| ZA (1) | ZA200608123B (fr) |
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